Canonical Allele Identifier: CA360425577

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119311T>A (hg19) ; chr5:g.90823494T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823494T>A , CM000667.2:g.90823494T>A	GRCh38
NC_000005.9:g.90119311T>A , CM000667.1:g.90119311T>A	GRCh37
NC_000005.8:g.90155067T>A	NCBI36
NG_007083.1:g.269695T>A
NG_007083.2:g.299151T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16266T>A MANE Select	ENSP00000384582.2:p.Asp5422Glu
ENST00000425867.3:c.5220T>A	ENSP00000392618.3:p.Asp1740Glu
ENST00000638510.1:n.3533T>A
ENST00000639431.1:c.265+147285T>A	ENSP00000491057.1:n.265+147285T>A
ENST00000640061.1:n.128+1312T>A
ENST00000640407.1:c.2676T>A	ENSP00000491425.1:p.Asp892Glu
ENST00000405460.6:c.16266T>A	ENSP00000384582.2:p.Asp5422Glu
ENST00000425867.2:c.3249T>A	ENSP00000392618.2:p.Asp1083Glu
NM_032119.3:c.16266T>A	NP_115495.3:p.Asp5422Glu
NR_003149.1:n.16279T>A
XM_011543675.1:c.16263T>A	XP_011541977.1:p.Asp5421Glu
XM_011543676.1:c.16185T>A	XP_011541978.1:p.Asp5395Glu
XM_011543677.1:c.13569T>A	XP_011541979.1:p.Asp4523Glu
NM_032119.4:c.16266T>A MANE Select	NP_115495.3:p.Asp5422Glu
XM_017009963.2:c.16287T>A	XP_016865452.1:p.Asp5429Glu
XM_017009964.2:c.16284T>A	XP_016865453.1:p.Asp5428Glu
XM_017009965.1:c.16284T>A	XP_016865454.1:p.Asp5428Glu
XM_017009966.2:c.16206T>A	XP_016865455.1:p.Asp5402Glu
XM_017009967.1:c.16191T>A	XP_016865456.1:p.Asp5397Glu
XM_017009968.2:c.16107T>A	XP_016865457.1:p.Asp5369Glu
XM_017009969.2:c.16287T>A	XP_016865458.1:p.Asp5429Glu
XM_017009972.1:c.9405T>A	XP_016865461.1:p.Asp3135Glu
XM_017009973.1:c.9384T>A	XP_016865462.1:p.Asp3128Glu
NR_003149.2:n.16282T>A